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Certain long non-coding RNAs in cashmere goats affect hair growth when treated with a specific growth factor.

The report expanded knowledge of MBTPS1-related disorders by identifying new symptoms.

KRT14 gene variants cause dermatopathia pigmentosa reticularis, affecting nails, teeth, and hair.

A new mutation linked to partial Androgen Insensitivity Syndrome and prostate cancer was found in a patient unhappy with their female gender assignment.

LMWP-PDGFA shows promise for improving hair health and treating hair loss with fewer side effects.

Two new proteins, hKAP1.6 and hKAP1.7, are found in the hair follicle cortex.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

CCL5 is important for the hair growth potential of human dermal papilla cells.

A new gene mutation causes vitamin D resistance and rickets, treatable with calcium therapy.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

The hr gene is linked to hair loss in Valle del Belice sheep.

A PKP1 gene mutation causes skin fragility and hair loss in Chesapeake Bay retriever puppies.

Overexpression of hurpin in mice leads to abnormal skin and higher skin cancer risk.

PRP injections may improve hair thickness and density in female hair loss patients.

PNU 157706 is a more effective treatment than finasteride for conditions caused by DHT, like enlarged prostate and hair loss.

Genetic variations in hair keratin proteins exist but don't significantly affect hair structure.

Mutations in the KRT16 gene can cause skin and nail disorders.

The research identified six functional hair keratin genes and four pseudogenes, providing insights into hair formation and gene organization.

Progeria, a disease that causes early aging, is linked to a gene mutation and helps us understand normal aging.

Pro-Ile could be used in cosmetics to improve skin, hair growth, and healing.

Scientists found genes linked to hair length in Brangus cattle that could help breed heat-tolerant cattle.

p21waf1/cip1 and p27kip1 help in hair follicle differentiation in rats.

The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.

PROTACs offer a new, precise way to treat cancer by breaking down harmful proteins.

Finasteride helps female-pattern hair loss.

A specific gene variant may increase the risk of developing Alopecia Areata.

The project developed and tested a method using plasma rich platelets to treat hair loss.

KRT2.13 gene is similar to KRT2.9 but not expressed in hair follicles.

A new genetic mutation in the CAST gene may link PLACK syndrome to alopecia areata.